Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1744297
ASPG
14 104102135 intron variant T/C snv 0.86 12
rs61997624
ASPG ; MIR203A
14 104116049 upstream gene variant C/T snv 0.12 2
rs33984773
ATP5MPL ; TDRD9
14 103927429 intron variant G/A snv 0.26 2
rs12587001
LOC105370708
14 104135840 upstream gene variant C/G;T snv 2